Objectives of Conference

Understand QbD fundamentals, including CQAs, risk assessment, and design space.

Learn practical implementation of QbD in formulation, analysis, and validation.

Navigate regulatory compliance with agencies like FDA, EMA, and ICH.

Explore global harmonization efforts in pharmaceutical quality standards.

Analyze real-world QbD case studies and industry best practices.

Dive into advanced QbD topics, including nanotechnology and continuous manufacturing.

Develop skills in statistical tools and risk assessment for QbD.

Embrace interdisciplinary collaboration between academia and industry.

Stay updated on future trends and innovations in pharmaceutical quality.

Network with experts, peers, and potential collaborators.

Participate in hands-on workshops for practical QbD experience.

Explore innovative projects and products through poster presentations.